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Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

PCOS is a common hormonal disorder in women that can be managed with lifestyle changes and various medications.

Notch signalling helps skin cells differentiate and prevents tumors.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

Altering SSAT affects fat metabolism and body fat in mice.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

New vitiligo treatments focus on controlling immune damage and restoring skin color.

Edar signaling is crucial for proper hair follicle development and function.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

Root hair growth in plants is a complex process controlled by many factors working together.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Female pattern hair loss is caused by multiple factors and while treatments like topical minoxidil, hormone therapy, and low-level light therapy can help, none can fully cure it.

A woman with severe hair loss was successfully treated with the drug adalimumab.

Mast cells likely promote skin scarring and fibrosis, but their exact role is still unclear.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

Alopecia areata is a chronic condition causing hair loss, with new treatments targeting the immune system showing promise.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

Mice with a virus similar to COVID-19 had skin damage, but a special treatment helped repair it.

Early recognition and treatment of tinea capitis are crucial to prevent severe scalp issues and prolonged therapy.

Menopause can cause hair thinning and texture changes due to hormonal and metabolic shifts.

Different causes of beard hair loss have various treatments, including medications, lifestyle changes, and procedures to stimulate hair growth.

The study concluded that people with Lichen Planopilaris have a more diverse scalp bacteria and different metabolic pathways compared to healthy individuals.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.